@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP794034.RAzIn2cMhdujmZGWHVqW6S-uD5uc0057AxBS6La72nDOQ
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP794034.RAzIn2cMhdujmZGWHVqW6S-uD5uc0057AxBS6La72nDOQ130_head
{
this:
np:hasAssertion
dgn-np:NP794034.RAzIn2cMhdujmZGWHVqW6S-uD5uc0057AxBS6La72nDOQ130_assertion
;
np:hasProvenance
dgn-np:NP794034.RAzIn2cMhdujmZGWHVqW6S-uD5uc0057AxBS6La72nDOQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP794034.RAzIn2cMhdujmZGWHVqW6S-uD5uc0057AxBS6La72nDOQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP794034.RAzIn2cMhdujmZGWHVqW6S-uD5uc0057AxBS6La72nDOQ130_assertion
a
np:Assertion
.
dgn-np:NP794034.RAzIn2cMhdujmZGWHVqW6S-uD5uc0057AxBS6La72nDOQ130_provenance
a
np:Provenance
.
dgn-np:NP794034.RAzIn2cMhdujmZGWHVqW6S-uD5uc0057AxBS6La72nDOQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP794034.RAzIn2cMhdujmZGWHVqW6S-uD5uc0057AxBS6La72nDOQ130_assertion
{
miriam-gene:4846
a
ncit:C16612
.
lld:C1852242
a
ncit:C7057
.
dgn-gda:DGNf24fef847333509c596be8ec80c24a5a
sio:SIO_000628
miriam-gene:4846
,
lld:C1852242
;
a
sio:SIO_001121
.
}
dgn-np:NP794034.RAzIn2cMhdujmZGWHVqW6S-uD5uc0057AxBS6La72nDOQ130_provenance
{
dgn-np:NP794034.RAzIn2cMhdujmZGWHVqW6S-uD5uc0057AxBS6La72nDOQ130_assertion
dcterms:description
"[The precise mechanism of NAION occurrence has not been elucidated yet; since NAION may occur when a compromised watershed microcirculation is combined with insufficient autoregulation of systematic circulation, other alterations in the eNOS gene or polymorphism of genes involved in systematic circulation may be associated with NAION occurrence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:21073768
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP794034.RAzIn2cMhdujmZGWHVqW6S-uD5uc0057AxBS6La72nDOQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:07+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}